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拉考沙胺与已有的抗癫痫药物在小鼠 6-羟色胺癫痫模型中的协同作用。

Synergism of lacosamide with established antiepileptic drugs in the 6-Hz seizure model in mice.

机构信息

Odessa State Medical University, Odessa, Ukraine.

出版信息

Epilepsia. 2013 Jul;54(7):1167-75. doi: 10.1111/epi.12237. Epub 2013 Jun 10.

DOI:10.1111/epi.12237
PMID:23750855
Abstract

PURPOSE

Lacosamide (LCM, Vimpat) is an anticonvulsant with a unique mode of action. This provides lacosamide with the potential to act additively or even synergistically with other antiepileptic drugs (AEDs). The objective of this study was to determine the presence of such interactions by isobolographic analysis.

METHODS

The anticonvulsant effect of LCM in combination with other AEDs including carbamazepine (CBZ), phenytoin (PHT), valproate (VPA), lamotrigine (LTG), topiramate (TPM), gabapentin (GBP), and levetiracetam (LEV) at fixed dose ratios of 1:3, 1:1, and 3:1, was evaluated in the 6-Hz-induced seizure model in mice. In addition, the impact of the combinations of LCM with the other AEDs on motor coordination was assessed in the rotarod test. Finally, AED concentrations were measured in blood and brain to evaluate potential pharmacokinetic drug interactions.

KEY FINDINGS

All studied AEDs produced dose-dependent anticonvulsant effects against 6-Hz-induced seizures. Combinations of LCM with CBZ, LTG, TPM, GBP, or LEV were synergistic. All other LCM/AED combinations displayed additive effects with a tendency toward synergism. Furthermore, no enhanced adverse effects were observed in the rotarod test by combining LCM with other AEDs. No pharmacokinetic interactions were seen on brain AED concentrations. Coadministration of LCM and TPM led to an increase in plasma levels of LCM, whereas the plasma concentration of PHT was increased by coadministration of LCM.

SIGNIFICANCE

The synergistic anticonvulsant interaction of LCM with various AEDs, without exacerbation of adverse motor effects, highlights promising properties of LCM as add-on therapy for drug refractory epilepsy.

摘要

目的

拉科酰胺(LCM,Vimpat)是一种具有独特作用机制的抗癫痫药。这使拉科酰胺有可能与其他抗癫痫药(AEDs)相加或协同作用。本研究的目的是通过等辐射分析确定这种相互作用的存在。

方法

在小鼠 6-Hz 诱导的惊厥模型中,评估了拉科酰胺与其他 AEDs(包括卡马西平(CBZ)、苯妥英(PHT)、丙戊酸(VPA)、拉莫三嗪(LTG)、托吡酯(TPM)、加巴喷丁(GBP)和左乙拉西坦(LEV))以固定剂量比 1:3、1:1 和 3:1 联合使用的抗惊厥作用。此外,还在旋转棒试验中评估了拉科酰胺与其他 AED 联合对运动协调的影响。最后,测量了血液和大脑中的 AED 浓度,以评估潜在的药代动力学药物相互作用。

主要发现

所有研究的 AED 对 6-Hz 诱导的惊厥均产生剂量依赖性抗惊厥作用。拉科酰胺与 CBZ、LTG、TPM、GBP 或 LEV 的联合具有协同作用。所有其他 LCM/AED 联合均表现出相加作用,具有协同作用的趋势。此外,拉科酰胺与其他 AED 联合使用在旋转棒试验中未观察到增强的不良作用。在大脑 AED 浓度上未观察到药代动力学相互作用。拉科酰胺与 TPM 联合给药导致拉科酰胺的血浆水平升高,而拉科酰胺与 PHT 联合给药导致 PHT 的血浆浓度升高。

意义

拉科酰胺与各种 AED 协同抗惊厥作用,无不良运动作用加重,突显了拉科酰胺作为药物难治性癫痫附加治疗的有前途的特性。

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